Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:16454205rdf:typepubmed:Citationlld:pubmed
pubmed-article:16454205lifeskim:mentionsumls-concept:C0010558lld:lifeskim
pubmed-article:16454205lifeskim:mentionsumls-concept:C0016693lld:lifeskim
pubmed-article:16454205lifeskim:mentionsumls-concept:C0038818lld:lifeskim
pubmed-article:16454205lifeskim:mentionsumls-concept:C0046100lld:lifeskim
pubmed-article:16454205lifeskim:mentionsumls-concept:C0033268lld:lifeskim
pubmed-article:16454205lifeskim:mentionsumls-concept:C0205214lld:lifeskim
pubmed-article:16454205lifeskim:mentionsumls-concept:C1702796lld:lifeskim
pubmed-article:16454205pubmed:issue1lld:pubmed
pubmed-article:16454205pubmed:dateCreated2006-2-3lld:pubmed
pubmed-article:16454205pubmed:abstractTextThe influence of complexation with hydroxypropyl-beta-cyclodextrin (HP-beta-CD) or beta-cyclodextrin (beta-CD) on the photo-induced production of free radicals by the sunscreen agents octyl-dimethylaminobenzoate (ODAB), oxybenzone (OB) and octyl-methoxycinnamate (OMC) was investigated. The formation of radical species during irradiation was detected by spin-trapping electron paramagnetic resonance (EPR) spectroscopy. 2,2,6,6-tetramethylpiperidine-1-oxyl, nitroxide radical (TEMPO) and 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) were used a spin-traps. Following the 4-h illumination with simulated sunlight, OB did not generate radicals. On the other hand, photoexcitation of solutions containing ODAB or OMC produced a marked decrease (>40%) of the TEMPO signal intensity, demonstrating the formation of carbon-centred radicals. In addition, the results obtained on irradiation of ODAB solutions containing DMPO as spin-trap indicated the generation of oxygen-centred radicals. Complexation of ODAB with HP-beta-CD and OMC with beta-CD markedly inhibited (>64%) the formation of free radicals generated by the sunscreens on exposure to simulated sunlight. Therefore, inclusion of ODAB and OMC into the cyclodextrin cavities minimizes their photosensitising potential.lld:pubmed
pubmed-article:16454205pubmed:languageenglld:pubmed
pubmed-article:16454205pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16454205pubmed:citationSubsetIMlld:pubmed
pubmed-article:16454205pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16454205pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16454205pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16454205pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16454205pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16454205pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16454205pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16454205pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16454205pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:16454205pubmed:statusMEDLINElld:pubmed
pubmed-article:16454205pubmed:monthJanlld:pubmed
pubmed-article:16454205pubmed:issn0031-7144lld:pubmed
pubmed-article:16454205pubmed:authorpubmed-author:MolinariAAlld:pubmed
pubmed-article:16454205pubmed:authorpubmed-author:ScaliaSSlld:pubmed
pubmed-article:16454205pubmed:authorpubmed-author:CasolariAAlld:pubmed
pubmed-article:16454205pubmed:authorpubmed-author:MaldottiAAlld:pubmed
pubmed-article:16454205pubmed:authorpubmed-author:TursilliRRlld:pubmed
pubmed-article:16454205pubmed:issnTypePrintlld:pubmed
pubmed-article:16454205pubmed:volume61lld:pubmed
pubmed-article:16454205pubmed:ownerNLMlld:pubmed
pubmed-article:16454205pubmed:authorsCompleteYlld:pubmed
pubmed-article:16454205pubmed:pagination41-5lld:pubmed
pubmed-article:16454205pubmed:dateRevised2007-1-29lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:meshHeadingpubmed-meshheading:16454205...lld:pubmed
pubmed-article:16454205pubmed:year2006lld:pubmed
pubmed-article:16454205pubmed:articleTitleInfluence of complexation with cyclodextrins on photo-induced free radical production by the common sunscreen agents octyl-dimethylaminobenzoate and octyl-methoxycinnamate.lld:pubmed
pubmed-article:16454205pubmed:affiliationDipartimento di Chimica, Università di Ferrara, Ferrara, Italy.lld:pubmed
pubmed-article:16454205pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16454205pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed